Protein Profiling of Orthosiphon stamineus Embryogenic Callus using Liquid Chromatography Coupled with Tandem-Mass Spectrometry (LC-MS/MS)

Q4 Agricultural and Biological Sciences
D. Mamat, Z. Rahmat, Tsun-Thai Chai, F. Manan
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引用次数: 1

Abstract

Orthosiphon stamineus is one of the most prominent medicinal herbs widely grown in Southeast Asia. Propagation of O. stamineus using tissue culture technique helps to rapidly produce samples for research purposes, increase the production of secondary metabolites and is considered as one of the strategies in plant genetic improvement. Despite vast information on O. stamineus pharmacological properties, the protein profile of this species is currently underexplored. In the present study, proteins expressed in embryogenic callus developed from O. stamineus leaves in Murashige and Skoog medium supplemented with 1-naphthaleneacetic acid (NAA) and 2,4-dichlorophenoxyacetic acid (2,4-D) were identified via Liquid chromatography- tandem mass spectrometry (LC-MS/MS). The presence of embryogenic callus was confirmed with microscope observation and Evan Blue assay. Using this proteomic approach, we identified peptides that represent 22 proteins localized to different cell compartments and involved in various biological and metabolic functions in plants. This finding is useful to improve our understanding of protein functions, thus their future applications could be further explored. Keywords: Embryogenic, Callus, Herb, Orthosiphon stamineus, Proteins
液相色谱-串联质谱法(LC-MS/MS)对正虹吸管stamineus胚性愈伤组织的蛋白质分析
正虹吸管是东南亚地区广泛种植的最著名的药材之一。利用组织培养技术繁殖O.stamineus有助于快速生产用于研究目的的样品,增加次生代谢产物的产生,被认为是植物遗传改良的策略之一。尽管有大量关于O.stamineus药理学特性的信息,但该物种的蛋白质图谱目前尚未得到充分的探索。本研究采用液相色谱-串联质谱法(LC-MS/MS)对在添加1-萘乙酸(NAA)和2,4-二氯苯氧基乙酸(2,4-D)的Murashige和Skoog培养基中由大麦叶片发育而成的胚性愈伤组织中表达的蛋白质进行了鉴定。通过显微镜观察和埃文蓝试验证实了胚性愈伤组织的存在。使用这种蛋白质组学方法,我们鉴定了代表22种蛋白质的肽,这些蛋白质定位于不同的细胞区室,并参与植物的各种生物和代谢功能。这一发现有助于提高我们对蛋白质功能的理解,从而进一步探索其未来的应用。关键词:胚性,愈伤组织,草本植物,正虹吸管雄蕊,蛋白质
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来源期刊
Journal of Tropical Life Science
Journal of Tropical Life Science Environmental Science-Ecology
CiteScore
1.00
自引率
0.00%
发文量
46
审稿时长
12 weeks
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